Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
| Chrom. | Start | End | TF Name | Source | Predicted site? | Tissue/Cell line | id | More |
|---|---|---|---|---|---|---|---|---|
| chr12 | 122771781 | 122771791 | TEAD1 | JASPAR | yes | 82491594 | ||
| chr12 | 122771781 | 122771791 | TEAD4 | JASPAR | yes | 82491595 | ||
| chr12 | 122771815 | 122771829 | FOXF2 | JASPAR | yes | 82491596 | ||
| chr12 | 122771815 | 122771830 | FOXP1 | JASPAR | yes | 82491597 | ||
| chr12 | 122771816 | 122771830 | POU4F1 | JASPAR | yes | 82491598 | ||
| chr12 | 122771816 | 122771831 | FOXA1 | JASPAR | yes | 82491599 | ||
| chr12 | 122771817 | 122771828 | FOXB1 | JASPAR | yes | 82491600 | ||
| chr12 | 122771817 | 122771828 | FOXC1 | JASPAR | yes | 82491601 | ||
| chr12 | 122771817 | 122771828 | PROP1 | JASPAR | yes | 82491602 | ||
| chr12 | 122771817 | 122771829 | FOXC2 | JASPAR | yes | 82491603 | ||
| chr12 | 122771818 | 122771830 | FOXI1 | JASPAR | yes | 82491604 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr12 | 122771826 | rs188475918 | T | C |
|
2957618 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12 | 122688090 | 122693499 | + | B3GNT4 | ENSG00000176383.8 | 122688090 | 0.94 | 1.0 | 12641 | 16309 | |
| chr12 | 122692210 | 122712081 | - | DIABLO | ENSG00000184047.11 | 122712081 | 0.74 | 0.93 | 12642 | 40300 | |
| chr12 | 122692326 | 122750970 | - | RP11-512M8.5 | ENSG00000256861.1 | 122750970 | 0.94 | 0.85 | 12643 | 79189 | |
| chr12 | 122714111 | 122751068 | - | VPS33A | ENSG00000139719.5 | 122751068 | 0.61 | 0.97 | 12644 | 79287 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|